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Journal Abstract Search


54 related items for PubMed ID: 2020300

  • 21. Monozygotic twins discordant for primary lateral sclerosis.
    Sorenson EJ.
    Amyotroph Lateral Scler; 2006 Jun; 7(2):123-5. PubMed ID: 16753978
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  • 22. Multiple sclerosis and amyotrophic lateral sclerosis; etiologic significance of recent epidemiologic and genetic studies.
    KURLAND LT, MULDER DW, WESTLUND KB.
    N Engl J Med; 1955 Apr 21; 252(16):649-53. PubMed ID: 14370401
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  • 23. Multiple sclerosis and amyotrophic lateral sclerosis (concluded); etiologic significance of recent epidemiologic and genetic studies.
    KURLAND LT, MULDER DW, WESTLUND KB.
    N Engl J Med; 1955 Apr 28; 252(17):697-702. PubMed ID: 14370411
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  • 25. Pathogenic mechanisms in familial amyotrophic lateral sclerosis due to mutation of Cu, Zn superoxide dismutase.
    Gurney ME, Cutting FB, Zhai P, Andrus PK, Hall ED.
    Pathol Biol (Paris); 1996 Jan 28; 44(1):51-6. PubMed ID: 8734301
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  • 26. [Contribution to the familial occurrence of amyotrophic lateral sclerosis. Studies on amyotrophic lateral sclerosis. VI].
    SERCL M, KOVARIK J.
    Cesk Neurol; 1960 Oct 28; 23():406-11. PubMed ID: 13750173
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  • 28. [Molecular genetic analysis of amyotrophic lateral sclerosis/parkinsonism-dementia complex (ALS/PDC) in the Kii peninsula].
    Hara K, Kuwano R, Miyashita A, Kokubo Y, Sasaki R, Nakahara Y, Goto J, Nishizawa M, Kuzuhara S, Tsuji S.
    Rinsho Shinkeigaku; 2007 Nov 28; 47(11):974-6. PubMed ID: 18210852
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  • 29. [HLA and amyotrophic lateral sclerosis (author's transl)].
    Seignalet J, Cadilhac J, Lapinski H.
    Sem Hop; 2007 Nov 28; 55(23-26):1239-40. PubMed ID: 227116
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  • 30. A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2.
    Hadano S, Hand CK, Osuga H, Yanagisawa Y, Otomo A, Devon RS, Miyamoto N, Showguchi-Miyata J, Okada Y, Singaraja R, Figlewicz DA, Kwiatkowski T, Hosler BA, Sagie T, Skaug J, Nasir J, Brown RH, Scherer SW, Rouleau GA, Hayden MR, Ikeda JE.
    Nat Genet; 2001 Oct 28; 29(2):166-73. PubMed ID: 11586298
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  • 35. An inherited disease similar to amyotrophic lateral sclerosis with a pattern of posterior column involvement. An intermediate form?
    ENGEL WK, KURLAND LT, KLATZO I.
    Brain; 1959 Jun 28; 82():203-20. PubMed ID: 13849712
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  • 38. Linkage of a gene causing familial amyotrophic lateral sclerosis to chromosome 21 and evidence of genetic-locus heterogeneity.
    Siddique T, Figlewicz DA, Pericak-Vance MA, Haines JL, Rouleau G, Jeffers AJ, Sapp P, Hung WY, Bebout J, McKenna-Yasek D.
    N Engl J Med; 1991 May 16; 324(20):1381-4. PubMed ID: 2020294
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  • 40. A molecular genetic approach to amyotrophic lateral sclerosis.
    Siddique T, Hu P, Hentati A, Deng G, Hung WY, McInnis MG, Warren AC, Rimmler J, Antonarakis S, Pericak-Vance MA.
    Int J Neurol; 1991 May 16; 25-26():60-9. PubMed ID: 11980064
    [Abstract] [Full Text] [Related]


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